The Associate Project Director, GRAPS leads complex projects across Global Regulatory Affairs and Global Patient Safety, ensuring disciplined execution and strategic alignment.
Play a high-impact role as the Associate Director of Medical Affairs, leading strategies and partnerships across the APAC region to advance innovative treatments.
The Associate Director, Global Medical Writing (Publications) will write and edit scientific publications related to clinical trials in endocrine indications, collaborating with various internal and external stakeholders.
As an Associate Director in Global Scientific Training, you will enhance scientific training programs for Medical Affairs teams, fostering a culture of continuous learning and collaboration.
The Sr. Clinical Trial Manager is responsible for overseeing Ascendis' global and regional clinical trials, ensuring compliance and effective collaboration among cross-functional teams.
The Medical Assessment and Signal Detection Lead is responsible for reviewing and approving Individual Case Safety Reports (ICSRs) and performing signal detection activities in collaboration with program safety leads.
The Program Safety Lead will define safety strategies, ensure compliance with pharmacovigilance regulations, and oversee safety activities for Ascendis Pharma's endocrinology pipeline.
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